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Page 1
Factor X deficiency.
Menegatti M, Peyvandi F. Menegatti M, et al. Semin Thromb Hemost. 2009 Jun;35(4):407-15. doi: 10.1055/s-0029-1225763. Epub 2009 Jul 13. Semin Thromb Hemost. 2009. PMID: 19598069 Review.
Factor X deficiency.
Uprichard J, Perry DJ. Uprichard J, et al. Blood Rev. 2002 Jun;16(2):97-110. doi: 10.1054/blre.2002.0191. Blood Rev. 2002. PMID: 12127953 Review.
The clinical phenotype is of a variable bleeding tendency. Homozygous factor X deficiency has an incidence of 1:1,000,000 in the general population. Heterozygotes are often clinically asymptomatic. Acquired factor X deficiency is rare, bu …
The clinical phenotype is of a variable bleeding tendency. Homozygous factor X deficiency has an incidence of 1:1,000,0 …
Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiency.
Peyvandi F, Auerswald G, Austin SK, Liesner R, Kavakli K, Álvarez Román MT, Millar CM. Peyvandi F, et al. Blood Rev. 2021 Nov;50:100833. doi: 10.1016/j.blre.2021.100833. Epub 2021 Apr 27. Blood Rev. 2021. PMID: 34024682 Free article. Review.
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. ...Evidence-based guidelines and reviews on factor X deficiency are generally limited to publications covering a range of rare bleeding disorders. ...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. ...Evidence-based guidelines and
Factor X.
Jackson CM. Jackson CM. Prog Hemost Thromb. 1984;7:55-109. Prog Hemost Thromb. 1984. PMID: 6397768 Review. No abstract available.
Biochemistry of factor X.
Hertzberg M. Hertzberg M. Blood Rev. 1994 Mar;8(1):56-62. doi: 10.1016/0268-960x(94)90007-8. Blood Rev. 1994. PMID: 8205010 Review.
62 results